Identification of a Novel Dentin Matrix Protein-1 (DMP-1) Mutation and Dental Anomalies in a Kindred with Autosomal Recessive Hypophosphatemia

Lignende værker

• Long-Term Clinical Outcome and Carrier Phenotype in Autosomal Recessive Hypophosphatemia Caused by a Novel DMP1 Mutation
  af: Mäkitie, Outi, et al.
  Udgivet: (2010)
• Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib
  af: Turan, Serap, et al.
  Udgivet: (2010)
• DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
  af: Lorenz-Depiereux, Bettina, et al.
  Udgivet: (2006)
• Constitutional Growth Delay Pattern of Growth in Velo−Cardio−Facial Syndrome: Longitudinal follow up and final height of two cases
  af: Turan, Serap, et al.
  Udgivet: (2008)
• Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatasez-scores in Different Types of Rickets
  af: Turan, Serap, et al.
  Udgivet: (2011)